• A unique phenotype of 2q24.3-2q32.1 duplication: early infantile epileptic encephalopathy without mesomelic dysplasia
• Cytogenetics of hepatoblastoma
• Duplication at chromosome 2q31.1-q31.2 in a family presenting syndactyly and nystagmus
• Heterogeneity of a Constitutional Complex Chromosomal Rearrangement in 2q
• Interstitial duplication of 2q32.1-q33.3 in a patient with epilepsy, developmental delay, and autistic behavior
• Mesomelic dysplasia Kantaputra type is associated with duplications of the HOXD locus on chromosome 2q
• Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis
• Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10p
• Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement
• Phenotypic and molecular characterization of partial trisomy 2q resulting from insertion-duplication in chromosome 18q: a case report and review of literature
• Prenatal Diagnosis and Molecular Cytogenetic Characterization of Copy Number Variations on 4p15.2p16.3, Xp22.31, and 12p11.1q11 in a Fetus with Ultrasound Anomalies: A Case Report and Literature Review
• Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results
• Pure distal trisomy 2q: a rare chromosomal abnormality with recognizable phenotype
• Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder
• Terminal 2q deletion and partial trisomy chromosome 15q: a clinical and cytogenetic study